Prasad Anil, Kumar Binod, Jena Sanghamitra, Mishra Minakshi, Sarkar Nilanjan
Pathology, Tata Main Hospital, Jamshedpur, IND.
Dermatology, Tata Main Hospital, Jamshedpur, IND.
Cureus. 2024 Dec 6;16(12):e75244. doi: 10.7759/cureus.75244. eCollection 2024 Dec.
We report a 37-year-old male patient who had nonbilious vomiting, no passage of flatus, and recurring abdominal pain. This patient had de novo intestinal myeloid sarcoma (MS), a rare and chameleonic presentation of acute leukemia of myeloid origin. The initial diagnostic evaluation suggested Koch's abdomen, and surgical excision of the bowel was performed with a clinical suspicion of Koch's or lymphoma. However, following extensive evaluation, it was diagnosed as chloroma. The rarity of intestinal MS without a pre-existing hematolymphoid malignancy presents a substantial diagnostic challenge, as few cases are documented in the literature.
我们报告了一名37岁男性患者,他出现了非胆汁性呕吐、无排气以及反复腹痛的症状。该患者患有原发性肠道髓系肉瘤(MS),这是一种起源于髓系的急性白血病的罕见且多变的表现形式。最初的诊断评估提示为科赫氏病,临床怀疑为科赫氏病或淋巴瘤而进行了肠道手术切除。然而,经过广泛评估后,诊断为绿色瘤。无先前血液淋巴系统恶性肿瘤的肠道MS非常罕见,这带来了巨大的诊断挑战,因为文献中记载的病例很少。